1. A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf–Hirschhorn syndrome. Issue 1 (15th November 2013) Authors: Terrone, Gaetano; Cappuccio, Gerarda; Genesio, Rita; Esposito, Annalisa; Fiorentino, Valeria; Riccitelli, Marina; Nitsch, Lucio; Brunetti‐Pierri, Nicola; Del Giudice, Ennio Journal: American journal of medical genetics Issue: Volume 164:Issue 1(2014.) Page Start: 190 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗